Evidence map›Paper›PMID 39227721›Full record

ArticleNature methods2024

Mapping cellular interactions from spatially resolved transcriptomics data.

James Zhu, Yunguan Wang, Woo Yong Chang, Alicia Malewska, Fabiana Napolitano, Jeffrey C Gahan, Nisha Unni, Min Zhao, Rongqing Yuan, Fangjiang Wu and 15 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature methods, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors.

James Zhu *Quantitative Biomedical Research Center, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0003-2713-1839
Yunguan Wang *Quantitative Biomedical Research Center, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Woo Yong Chang *Quantitative Biomedical Research Center, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-7129-5016
Alicia MalewskaDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Fabiana NapolitanoHarold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-2463-8952
Jeffrey C GahanDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Nisha UnniDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Min ZhaoDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Rongqing YuanQuantitative Biomedical Research Center, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Fangjiang WuQuantitative Biomedical Research Center, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Lauren YueQuantitative Biomedical Research Center, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Lei GuoQuantitative Biomedical Research Center, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Zhuo ZhaoDepartment of Computer Science and Engineering, University of Notre Dame, Notre Dame, IN, USA.
Danny Z ChenDepartment of Computer Science and Engineering, University of Notre Dame, Notre Dame, IN, USA.ORCID http://orcid.org/0000-0001-6565-2884
Raquibul HannanDepartment of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Siyuan ZhangDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0003-0910-3666
Guanghua XiaoQuantitative Biomedical Research Center, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0001-9387-9883
Ping MuDepartment of Molecular Biology, UT Southwestern Medical Center, Dallas, TX, USA.
Ariella B HankerHarold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-8655-8341
Douglas StrandDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Carlos L ArteagaHarold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Neil DesaiDepartment of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Xinlei WangDepartment of Mathematics, University of Texas at Arlington, Arlington, TX, USA. xinlei.wang@uta.edu.ORCID http://orcid.org/0000-0002-8561-6511
Yang XieQuantitative Biomedical Research Center, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA. yang.xie@utsouthwestern.edu.ORCID http://orcid.org/0000-0001-9456-1762
Tao WangQuantitative Biomedical Research Center, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA. tao.wang@utsouthwestern.edu.ORCID http://orcid.org/0000-0002-4355-149X

Funding

UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HEYMACH, JOHN V. · 1996 to 2024
$57.4M
UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Kathryn Ann O'Donnell · 2010 to 2026
$53.7M
Bedside to bench resources for lower urinary tract researchRC2DK129994 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Douglas William Strand, CHAD M. VEZINA · 2022 to 2026
$5.0M
Neural Niche in Promoting Brain Metastatic Tumor ProgressionR01CA255064 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI ZHANG, SIYUAN · 2021 to 2025
$2.3M
Notch-mediated 5ARI resistance in human BPHR01DK115477 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI STRAND, DOUGLAS WILLIAM · 2018 to 2022
$1.9M
Applying deep learning to predict T cell receptor binding specificity of neoantigens and response to checkpoint inhibitorsR01CA258584 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI WANG, TAO, WANG, XINLEI · 2021 to 2025
$1.4M
Interstitial fibroblasts drive prostate branching morphogenesisR01DK135535 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Douglas William Strand · 2023 to 2026
$1.4M
Cancer Prevention and Research Institute of Texas (Cancer Prevention Research Institute of Texas) RP190208Cancer Prevention and Research Institute of Texas (Cancer Prevention Research Institute of Texas) RP230363Cancer Prevention and Research Institute of Texas (Cancer Prevention Research Institute of Texas) RR170061Cancer Prevention and Research Institute of Texas (Cancer Prevention Research Institute of Texas) RR220024NCI NIH HHS P50 CA070907NCI NIH HHS R01 CA258584U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01CA255064U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01CA258584U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01DK115477U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01DK135535U.S. Department of Health & Human Services | National Institutes of Health (NIH) RC2DK129994
6 · The paper itself

Abstract

Cell-cell communication (CCC) is essential to how life forms and functions. However, accurate, high-throughput mapping of how expression of all genes in one cell affects expression of all genes in another cell is made possible only recently through the introduction of spatially resolved transcriptomics (SRT) technologies, especially those that achieve single-cell resolution. Nevertheless, substantial challenges remain to analyze such highly complex data properly. Here, we introduce a multiple-instance learning framework, Spacia, to detect CCCs from data generated by SRTs, by uniquely exploiting their spatial modality. We highlight Spacia's power to overcome fundamental limitations of popular analytical tools for inference of CCCs, including losing single-cell resolution, limited to ligand-receptor relationships and prior interaction databases, high false positive rates and, most importantly, the lack of consideration of the multiple-sender-to-one-receiver paradigm. We evaluated the fitness of Spacia for three commercialized single-cell resolution SRT technologies: MERSCOPE/Vizgen, CosMx/NanoString and Xenium/10x. Overall, Spacia represents a notable step in advancing quantitative theories of cellular communications.

Indexed as

Cell CommunicationGene Expression ProfilingSingle-Cell AnalysisTranscriptomeAnimalsHumans

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.